Preparation of an electrophilic glycine cation equivalent and its reaction with heteroatom nucleophiles

Martin J. O'Donnell, William D. Bennett, Robin L Polt

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

A variety of heteroatom substituted Schiff base amino esters 4 - 7 are prepared either from the benzophenone imine of glycine ethyl ester (3) or by reaction of acetate 4 with heteroatom nucleophiles.

Original languageEnglish (US)
Pages (from-to)695-698
Number of pages4
JournalTetrahedron Letters
Volume26
Issue number6
DOIs
StatePublished - 1985
Externally publishedYes

Fingerprint

Nucleophiles
Imines
Schiff Bases
Glycine
Cations
Esters
Acetates
glycine ethyl ester
benzophenone

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Preparation of an electrophilic glycine cation equivalent and its reaction with heteroatom nucleophiles. / O'Donnell, Martin J.; Bennett, William D.; Polt, Robin L.

In: Tetrahedron Letters, Vol. 26, No. 6, 1985, p. 695-698.

Research output: Contribution to journalArticle

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